PAIN RELIEVING PATCH ULTRA STRENGTH- menthol patch

Pain Relieving Patch by

Drug Labeling and Warnings

Pain Relieving Patch by is a Otc medication manufactured, distributed, or labeled by Walgreen Co.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Menthol 5%

PURPOSE

Purpose

Topical Analgesic

INDICATIONS & USAGE

Uses

Temporarily relieves minor aches and pains of muscles and joints associated with:

• arthritis
• simple backache
• strains
• sprains
• bruises
  

WARNINGS

Warnings
For external use only
If pregnant or breast-feeding, consult a healthcare professional before use

DO NOT USE

Do not use

• on wounds or damaged skin
• on a child under 12 years of age with arthritis-like conditions
  

ASK DOCTOR

Ask a doctor before use if you

• have redness over the affected area
  

WHEN USING

When using this product

• avoid contact with eyes and mucous membranes
• do not bandage tightly
• do not use with a heating pad or other heating devices

STOP USE

Stop use and ask a doctor if

• condition worsens
• excessive skin irritation occurs
• redness is present
• symptoms persist for more than 7 days or clear up and occur again within a few days
  

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions

• open pouch and remove patch
• if desired, cut patch to size
• peel off protective backing and apply sticky side to affected area
• adults and children 12 years of age and older apply to affected area no more than 3 to 4 times daily
• children under 12 years of age consult a doctor
  

STORAGE AND HANDLING

Other information

• store at room temperature
  

INACTIVE INGREDIENT

Inactive ingredients

alumina magnesioum metasilicate, BHT, castor oil, cellulose gum, disodium EDTA, gelatin, glycerin, isopropyl myristate, kaolin, methylparaben, PEG-4 stearate, polyacrylic acid, polysorbate 80, polyvinyl alcohol, purified water, sodium polyacrylate, tartaric acid, titanium dioxide.

QUESTIONS

Questions or comments?

1-800-WALGREENS (1-800-925-4733)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PAIN RELIEVING PATCH  ULTRA STRENGTH
menthol patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-0151
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Menthol (UNII: L7T10EIP3A) (Menthol - UNII:L7T10EIP3A)	Menthol	.05 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Silodrate (UNII: 9T3UU8T0QK)
Butylated Hydroxytoluene (UNII: 1P9D0Z171K)
Castor Oil (UNII: D5340Y2I9G)
Carboxymethylcellulose Sodium (UNII: K679OBS311)
Edetate Disodium (UNII: 7FLD91C86K)
Gelatin (UNII: 2G86QN327L)
Glycerin (UNII: PDC6A3C0OX)
Isopropyl Myristate (UNII: 0RE8K4LNJS)
Kaolin (UNII: 24H4NWX5CO)
Methylparaben (UNII: A2I8C7HI9T)
Peg-4 Stearate (UNII: J33E8608YN)
Polysorbate 80 (UNII: 6OZP39ZG8H)
Polyvinyl Alcohol (UNII: 532B59J990)
Water (UNII: 059QF0KO0R)
Tartaric Acid (UNII: W4888I119H)
Titanium Dioxide (UNII: 15FIX9V2JP)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-0151-01	4 in 1 BOX
1		1 g in 1 PATCH

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	08/15/2013

Labeler - Walgreen Co. (008965063)